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The mass spectrometric fragmentation of 1-(benzyloxycarbonyl)amino-2-alkyl/cyclo- alkyl thioacetates has been studied with the aid of mass-analysed ion kinetic energy spectrometry under electron impact ionization. All compounds show a tendency to eliminate a ketene, thioacetic acid, and benzyl carbamate molecule, or an acetyl and benzyloxy radicals. A thioester pyrolysis-type rearrangement under electron impact ionizations was observed.
The mass spectrometric fragmentation of 1- (benzyloxycarbonyl) amino-2-alkyl / cyclo-alkyl thioacetates has been studied with the aid of mass-analyzed ion kinetic energy spectrometry under electron impact ionization. All compounds show a tendency to eliminate a ketene, thioacetic acid, and benzyl carbamate molecule, or an acetyl and benzyloxy radicals. A thioester pyrolysis-type rearrangement under electron impact ionizations was observed.